Phenotypic and genetic analysis of a large family with migraine-associated vertigo

Headache

Volumn 48, Issue 10, 2008, Pages 1460-1467

  Lee, Hane ^b   Jen, Joanna C ^b   Cha, Yoon Hee ^b   Nelson, Stanley F ^b   Baloh, Robert W ^a,b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Female predominant; Identity by descent analysis; Migraine associated vertigo

Indexed keywords

AGED; ALLELE; ARTICLE; CHROMOSOME 11Q; CLINICAL ARTICLE; CLINICAL FEATURE; FAMILY; FEMALE; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC SUSCEPTIBILITY; GENOME; GENOTYPE; HUMAN; MALE; MIGRAINE; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SYMPTOM; VERTIGO;

ADULT; AGED; BRAIN CHEMISTRY; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENOTYPE; HUMANS; INHERITANCE PATTERNS; MALE; MIDDLE AGED; MIGRAINE DISORDERS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; VERTIGO; YOUNG ADULT;

EID: 56549084586     PISSN: 00178748     EISSN: 15264610     Source Type: Journal    
DOI: 10.1111/j.1526-4610.2007.01002.x     Document Type: Article

References (31)

1. Liveing E. On Megrim: Sick Headache and Some Allied Health Disorders: A Contribution to the Pathology of Nerve Storms. London : Churchill 1873.
2. Aragones JM, Fortes-Rego J, Fuste J, Cardozo A. Migraine: An alternative in the diagnosis of unclassified vertigo. Headache. 1993 33 : 125 128.
3. Kuritzky A, Ziegler DK, Hassanein R. Vertigo, motion sickness and migraine. Headache. 1981 21 : 227 231.
4. Neuhauser H, Leopold M, von Brevern M, Arnold G, Lempert T. The interrelations of migraine, vertigo, and migrainous vertigo. Neurology. 2001 56 : 436 441.
5. Savundra PA, Carroll JD, Davies RA, Luxon LM. Migraine-associated vertigo. Cephalalgia. 1997 17 : 505 510 discussion 487.
6. von Brevern M, Ta N, Shankar A, et al. Migrainous vertigo: Mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4. Headache. 2006 46 : 1136 1141.
7. Kayan A, Hood JD. Neuro-otological manifestations of migraine. Brain. 1984 107 : 1123 1142.
8. Mira E, Piacentino G, Lanzi G, Balottin U, Fazzi E. Benign paroxysmal vertigo in childhood: A migraine equivalent. ORL J Otorhinolaryngol Relat Spec. 1984 46 : 97 104.
9. Lanzi G, Balottin U, Fazzi E, Tagliasacchi M, Manfrin M, Mira E. Benign paroxysmal vertigo of childhood: A long-term follow-up. Cephalalgia. 1994 14 : 458 460.
10. Moretti G, Manzoni GC, Caffarra P, Parma M. "Benign recurrent vertigo" and its connection with migraine. Headache. 1980 20 : 344 346.
11. Slater R. Benign recurrent vertigo. J Neurol Neurosurg Psychiatry. 1979 42 : 363 367.
12. Baloh RW. Genes and migraine. Drugs Today (Barc). 2004 40 : 577 588.
13. Stewart WF, Lipton RB, Liberman J. Variation in migraine prevalence by race. Neurology. 1996 47 : 52 59.
14. Ophoff RA, Terwindt GM, Vergouwe MN, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell. 1996 87 : 543 552.
15. Dichgans M, Freilinger T, Eckstein G, et al. Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. Lancet. 2005 366 : 371 377.
16. De Fusco M, Marconi R, Silvestri L, et al. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. Nat Genet. 2003 33 : 192 196.
17. Devoto M, Lozito A, Staffa G, D'Alessandro R, Sacquegna T, Romeo G. Segregation analysis of migraine in 128 families. Cephalalgia. 1986 6 : 101 105.
18. Mochi M, Sangiorgi S, Cortelli P, et al. Testing models for genetic determination in migraine. Cephalalgia. 1993 13 : 389 394.
19. Russell MB, Iselius L, Olesen J. Inheritance of migraine investigated by complex segregation analysis. Hum Genet. 1995 96 : 726 730.
20. Headache Classification Committee of the International Headache Society. Classification and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia. 1988 8 (Suppl. 7 1 96.
21. Nelson SF, Merriman B. Detecting identical-by-descent DNA intervals between affected distant relatives using high-density SNP genotyping. In 55th Annual American Society of Human Genetics Meeting, Salt Lake City, UT, 2005.
22. Nelson SF, McCusker JH, Sander MA, Kee Y, Modrich P, Brown PO. Genomic mismatch scanning: A new approach to genetic linkage mapping. Nat Genet. 1993 4 : 11 18.
23. Sobel E, Lange K. Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet. 1996 58 : 1323 1337.
24. Neuhauser HK. Epidemiology of vertigo. Curr Opin Neurol. 2007 20 : 40 46.
25. Stewart WF, Lipton RB, Celentano DD, Reed ML. Prevalence of migraine headache in the United States. Relation to age, income, race, and other sociodemographic factors. JAMA. 1992 267 : 64 69.
26. Oh AK, Lee H, Jen JC, Corona S, Jacobson KM, Baloh RW. Familial benign recurrent vertigo. Am J Med Genet. 2001 100 : 287 291.
27. Brantberg K, Trees N, Baloh RW. Migraine-associated vertigo. Acta Otolaryngol. 2005 125 : 276 279.
28. Colson NJ, Lea RA, Quinlan S, MacMillan J, Griffiths LR. Investigation of hormone receptor genes in migraine. Neurogenetics. 2005 6 : 17 23.
29. Nyholt DR, Morley KI, Ferreira MA, et al. Genomewide significant linkage to migrainous headache on chromosome 5q21. Am J Hum Genet. 2005 77 : 500 512.
30. Wessman M, Kallela M, Kaunisto MA, et al. A susceptibility locus for migraine with aura, on chromosome 4q24. Am J Hum Genet. 2002 70 : 652 662.
31. Kaunisto MA, Kallela M, Hamalainen E, et al. Testing of variants of the MTHFR and ESR1 genes in 1798 Finnish individuals fails to confirm the association with migraine with aura. Cephalalgia. 2006 26 : 1462 1472.